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Showing 3901–3910 of 58596 articles for “Art. s. 8 and 239”
If the regional or central council is responsible for failing to comply with the time limit referred to in article R. 4234-36, the author of the complaint may ask the president of the national council…
During the conciliation meeting, the parties and, where applicable, their representatives are heard by the conciliator(s). A report of total or partial conciliation or a report of non-conciliation is…
If the complaint concerns one of the members of the regional council, this council may ask the president of the national council to designate another regional council to organise the conciliation.If t…
Any manufacturer having its registered office in France and who, in any Member State of the European Union or party to the Agreement on the European Economic Area, places class I medical devices or cu…
The declarations provided for in Articles L. 5211-3-1 and R. 5211-65 as well as the communication provided for in Article R. 5211-66 are made to the Agence nationale de sécurité du médicament et des p…
The content and methods of presentation of the declaration are laid down, on a proposal from the Director General of the Agence nationale de sécurité du médicament et des produits de santé, by order o…
…thorised representative, the importer, distributor or exporter of in vitro diagnostic medical devices. The same natural or legal person may declare several activities. The manufacturer or its authoris…
Manufacturers who place in vitro diagnostic medical devices on the French market and who do not have their registered office on the territory of a Member State of the European Union or a party to the…
The Director General of the Agence nationale de sécurité du médicament et des produits de santé is notified of any changes to the information contained in the declaration.
…the spinal cord, the peripheral nerves, their envelopes (skull, vertebro-discal column, meninges) and their vessels and requiring or likely to require a neurosurgical or radiosurgical procedure unde…
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